warnings
For external use only. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs.
MENOKIN 30 SECONDS GLOW AND CLEAR Gel SUNSCREEN MOISTURE
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- MENOKIN 30 SECONDS GLOW AND CLEAR Gel SUNSCREEN MOISTURE
- Generic name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
- Manufacturer
- Forest Avenue Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- edbfcf21-96c6-4519-8b08-f9b5ada7d1d7
- SPL ID
- 5747ce7f-2fa3-536e-e063-6394a90a7d25
- Version
- 2
- Effective date
- 2026-07-23
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:29:00
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M020 | openfda.application_number | |
| brand name | MENOKIN 30 SECONDS GLOW AND CLEAR Gel SUNSCREEN MOISTURE | openfda.brand_name | |
| generic name | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | openfda.generic_name | |
| manufacturer name | Forest Avenue Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 87507-001-01 | openfda.package_ndc |
| ndc | package | 87507-001-02 | openfda.package_ndc |
| ndc | package | 87507-001-03 | openfda.package_ndc |
| ndc | product | 87507-001 | openfda.product_ndc |
| ndc11 | package | 87507000103 | derived:openfda.package_ndc |
| ndc11 | package | 87507000102 | derived:openfda.package_ndc |
| ndc11 | package | 87507000101 | derived:openfda.package_ndc |
| spl id | 5747ce7f-2fa3-536e-e063-6394a90a7d25 | id | |
| spl set id | edbfcf21-96c6-4519-8b08-f9b5ada7d1d7 | set_id | |
| unii | 5A68WGF6WM | openfda.unii | |
| unii | V06SV4M95S | openfda.unii | |
| unii | G63QQF2NOX | openfda.unii | |
| unii | 4X49Y0596W | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.